NP-MRD: Showing NP-Card for {2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate (NP0198344)

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Record Information

Version

2.0

Created at

2022-09-04 16:46:50 UTC

Updated at

2022-09-04 16:46:50 UTC

NP-MRD ID

NP0198344

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate

Description

{2-[(2,3-Dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate belongs to the class of organic compounds known as o-xylenes. These are aromatic compounds that contain a o-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 2-positions. {2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate is found in Senecio glutinosus. Based on a literature review very few articles have been published on {2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
    6.6704    0.2374    1.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2720    0.6498    0.9013 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2662   -0.1954    0.7615 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6331   -1.6510    0.7855 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9088    0.2739    0.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7211    1.5330    0.5735 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7977   -0.5764    0.4447 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5087   -0.0734    0.2759 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2896    0.6516   -0.9775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    0.7924   -2.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4337    0.2501   -2.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3163    1.5489   -2.9922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8235    1.8143   -2.4432 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9279    1.3214   -1.2475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0863    1.4190   -0.3084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9022    0.1946   -0.2464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6531   -0.8947   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4621   -2.0020   -0.9315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5017   -1.9934   -0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7672   -0.9100    0.7862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9092   -0.9450    1.7576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9526    0.1973    0.6682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2351    1.3657    1.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8461   -0.3481    1.9908 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3402    1.1171    1.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9477   -0.4239    0.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0399    1.7264    0.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2061   -1.8887    1.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7586   -2.3117    0.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3162   -1.8816   -0.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1957   -0.9574    0.3806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3379    0.6019    1.1780 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2682    0.9003   -2.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4460    0.1054   -3.4971 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6075   -0.7672   -1.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7033    1.8201   -3.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7461    2.2837   -0.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7090    1.6452    0.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8304   -0.8496   -1.7360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2701   -2.8819   -1.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1463   -2.8802    0.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5172   -1.8515    1.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5563   -1.0551    2.7988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6037   -0.0802    1.6123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3126    1.4766    1.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6932    1.1939    2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9180    2.2985    1.0502 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 14 13  1  0
 13 12  1  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
 22 16  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  8 31  1  0
  8 32  1  0
 15 37  1  0
 15 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
 12 36  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
M  END


  Mrv1652309042218462D          

 23 24  0  0  0  0            999 V2000
   -0.8212    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078    2.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    1.1759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222   -0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846   -1.5291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4888   -1.5291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1019   -2.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8865   -1.8262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4996   -2.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3281   -3.1852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5434   -3.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3719   -4.2471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303   -2.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1457   -3.1430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198344

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OCC1=C(CC2=CC=CC(C)=C2C)OC=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O3/c1-6-13(2)20(21)23-12-18-15(4)11-22-19(18)10-17-9-7-8-14(3)16(17)5/h6-9,11H,10,12H2,1-5H3

> <INCHI_KEY>
KPKYGFYBRSEOLB-UHFFFAOYSA-N

> <FORMULA>
C20H24O3

> <MOLECULAR_WEIGHT>
312.409

> <EXACT_MASS>
312.172544633

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.71168729893799

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate

> <JCHEM_LOGP>
5.955230662333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.747337613150818

> <JCHEM_POLAR_SURFACE_AREA>
39.44

> <JCHEM_REFRACTIVITY>
94.1094

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
{2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.533   2.195   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.199   1.425   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.134   2.195   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.134   3.735   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.468   1.425   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.802   2.195   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       2.468  -0.115   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.802  -0.885   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.802  -2.425   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.556  -3.330   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.091  -2.854   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.032  -4.795   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.572  -4.795   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.048  -3.330   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.512  -2.854   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.657  -3.885   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.121  -3.409   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.266  -4.439   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.946  -5.946   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.481  -6.422   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.161  -7.928   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.337  -5.391   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.872  -5.867   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   16   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
{2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₄O₃

Average Mass

312.4090 Da

Monoisotopic Mass

312.17254 Da

IUPAC Name

{2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate

Traditional Name

{2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OCC1=C(CC2=CC=CC(C)=C2C)OC=C1C

InChI Identifier

InChI=1S/C20H24O3/c1-6-13(2)20(21)23-12-18-15(4)11-22-19(18)10-17-9-7-8-14(3)16(17)5/h6-9,11H,10,12H2,1-5H3

InChI Key

KPKYGFYBRSEOLB-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Senecio glutinosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-xylenes. These are aromatic compounds that contain a o-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 2-positions.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Xylenes

Direct Parent

o-Xylenes

Alternative Parents

Substituents

O-xylene
Fatty acid ester
Fatty acyl
Furan
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Heteroaromatic compound
Carboxylic acid ester
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Carbonyl group
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.96	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	39.44 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	94.11 m³·mol⁻¹	ChemAxon
Polarizability	35.71 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162969681

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate (NP0198344)

MOL for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

3D MOL for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

3D SDF for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

3D-SDF for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

PDB for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

3D PDB for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

SMILES for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

INCHI for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

Structure for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)

3D Structure for NP0198344 ({2-[(2,3-dimethylphenyl)methyl]-4-methylfuran-3-yl}methyl 2-methylbut-2-enoate)